Canonical Allele Identifier: PA2580407296
Gene: CEP41 HGNC NCBI
ClinVar RCV:
RCV002621130
ClinVar Variation:
1920652
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_061188.1:p.Asp322Gly
CA369286908
NM_018718.3:c.965A>G